254133005: Pachydermoperiostosis - familial (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Imaging finding\Bone densimetry abnormal\Bone density above reference range\Dysplasia with increased bone density\Pachydermoperiostosis - familial

\General finding of observation of patient\Procedure related finding\Bone density finding\Bone density above reference range\Dysplasia with increased bone density\Pachydermoperiostosis - familial

\Musculoskeletal finding\Bone finding\Bone density finding\Bone density above reference range\Dysplasia with increased bone density\Pachydermoperiostosis - familial
\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Pachydermoperiostosis - familial
\Musculoskeletal finding\Bone finding\Disorder of bone\Dysplasia with increased bone density\Pachydermoperiostosis - familial
\Musculoskeletal finding\Musculoskeletal disorder\Disorder of skeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Pachydermoperiostosis - familial
\Musculoskeletal finding\Musculoskeletal disorder\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Pachydermoperiostosis - familial
\Musculoskeletal finding\Musculoskeletal disorder\Disorder of skeletal system\Disorder of bone\Dysplasia with increased bone density\Pachydermoperiostosis - familial
\Musculoskeletal finding\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Pachydermoperiostosis - familial
\Musculoskeletal finding\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Pachydermoperiostosis - familial

\Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Pachydermoperiostosis - familial
\Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Pachydermoperiostosis - familial
\Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal system\Disorder of bone\Dysplasia with increased bone density\Pachydermoperiostosis - familial
\Disease\Disorder of body system\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Pachydermoperiostosis - familial
\Disease\Disorder of body system\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Pachydermoperiostosis - familial
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Pachydermoperiostosis - familial
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Pachydermoperiostosis - familial
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Pachydermoperiostosis - familial
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with increased bone density\Pachydermoperiostosis - familial
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Pachydermoperiostosis - familial

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

378305012 Pachydermoperiostosis - familial en Synonym Active Case insensitive SNOMED CT core

378306013 Familial hypertrophic osteoarthropathy en Synonym Active Case insensitive SNOMED CT core

644983015 Pachydermoperiostosis - familial (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Pachydermoperiostosis - familial	Occurrence	Congenital	true	Inferred relationship	Some	1
Pachydermoperiostosis - familial	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Pachydermoperiostosis - familial	Interprets	Bone density scan	true	Inferred relationship	Some	2
Pachydermoperiostosis - familial	Has interpretation	Above reference range	true	Inferred relationship	Some	2
Pachydermoperiostosis - familial	Is a	Congenital anomaly of skeletal bone	true	Inferred relationship	Some
Pachydermoperiostosis - familial	Is a	Multisystem disorder	false	Inferred relationship	Some
Pachydermoperiostosis - familial	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	1
Pachydermoperiostosis - familial	Finding site	Bone structure	false	Inferred relationship	Some	1
Pachydermoperiostosis - familial	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	1
Pachydermoperiostosis - familial	Occurrence	Congenital	false	Inferred relationship	Some	2
Pachydermoperiostosis - familial	Finding site	Bone structure	false	Inferred relationship	Some	2
Pachydermoperiostosis - familial	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	2
Pachydermoperiostosis - familial	Finding site	Bone structure	true	Inferred relationship	Some	1
Pachydermoperiostosis - familial	Occurrence	Congenital	false	Inferred relationship	Some
Pachydermoperiostosis - familial	Finding site	Skeletal system structure	false	Inferred relationship	Some	1
Pachydermoperiostosis - familial	Associated morphology	Dysplasia	true	Inferred relationship	Some	1
Pachydermoperiostosis - familial	Is a	Dysplasia with increased bone density	true	Inferred relationship	Some
Pachydermoperiostosis - familial	Is a	Multisystem disorder O-P	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
378305012	Pachydermoperiostosis - familial	en	Synonym	Active	Case insensitive	SNOMED CT core
378306013	Familial hypertrophic osteoarthropathy	en	Synonym	Active	Case insensitive	SNOMED CT core
644983015	Pachydermoperiostosis - familial (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core